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NDT Plus|May 19, 2015
Bilineal inheritance of type 1 autosomal dominant polycystic kidney disease (ADPKD) and recurrent fetal lossRamón Peces, Carlos Peces, Eliecer Coto, et al.Thescientificworldjournal|November 30, 2011
Giant bilateral renal angiomyolipomas and lymphangioleiomyomatosis presenting after two successive pregnancies successfully treated with surgery and rapamycinRamón Peces, Emilio Cuesta-López, Carlos Peces, et al.BMC Medical Genetics|September 2, 2017
Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case reportRamón Peces, Sara Afonso, Carlos Peces, et al.International Urology and Nephrology|December 31, 2009
Massive gastric dilatation and anuria resolved with naso-gastric tube decompressionRamón Peces, Cristina Vega, Carlos Peces, et al.Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|March 20, 2012
Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuriaRamón Peces, Ana Aguilar, Cristina Vega, et al.Diagnostic Pathology|August 5, 2008
Serendipia: Castilla-La Mancha telepathology networkCarlos Peces, Marcial García-Rojo, José Sacristán, et al.NDT Plus|May 8, 2015
Sacral radicular cysts in autosomal dominant polycystic kidney diseaseRamón Peces, Carlos Peces, Virginia Pérez-Dueñas, et al.International Urology and Nephrology|July 24, 2012
A novel and de novo deletion in the OCRL1 gene associated with a severe form of Lowe syndromeRamón Peces, Carlos Peces, Erika de Sousa, et al.NDT Plus|May 8, 2015
Rapamycin reduces kidney volume and delays the loss of renal function in a patient with autosomal-dominant polycystic kidney diseaseRamón Peces, Carlos Peces, Virginia Pérez-Dueñas, et al.World Journal of Gastroenterology|January 27, 2006
Autosomal dominant polycystic liver disease in a family without polycystic kidney disease associated with a novel missense protein kinase C substrate 80K-H mutationRamón Peces, Joost P H Drenth, Rene H M Te Morsche, et al.Pageof 2